US10532124B2ActiveUtilityPatentIndex 49
Water soluble farnesol analogs and their use
Est. expiryDec 27, 2032(~6.5 yrs left)· nominal 20-yr term from priority
C07C 69/007C07C 33/02A61L 15/44A61L 15/20A61L 15/62C07C 43/15C07C 43/178A61L 2300/404A61L 2300/22C07C 69/67C07C 69/40C07H 3/02C07C 43/188C07C 43/1785A61L 2300/232A61F 13/8405C07C 69/73
49
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17
Claims
Abstract
Farnesol analogs, along with their related products (e.g., treatment compositions, wipes, absorbent articles, etc.) and their methods of formation, are provided. The farnesol analog includes a hydrophilic end group (e.g., a hydroxyl end group or a carboxylic acid end group) attached to farnesol via a covalent linkage (e.g., an ester group or an ether group).
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A farnesol analog comprising a hydrophilic end group attached to farnesol via a covalent linkage, wherein the hydrophilic end group defines a hydroxyl end group, and wherein the covalent linkage comprises an ester group or an ether group, wherein the farnesol analog comprises one of the structures:
where n is an integer from 1 to 8; m is an integer from 1 to 8; and p is an integer from 1 to 100.
2. The farnesol analog as in claim 1 , wherein the covalent linkage comprises an ester group.
3. The farnesol analog as in claim 1 , wherein n is 2, 3, or 4.
4. The farnesol analog as in claim 3 , wherein the hydrophilic end group comprises an ester group.
5. The farnesol analog as in claim 1 , wherein n is 2, 3, or 4; and wherein m is 2, 3, or 4.
6. The farnesol analog as in claim 1 , wherein the covalent linkage comprises an ether group, and wherein the hydrophilic end group defines a hydroxyl end group.
7. The farnesol analog as in claim 1 , wherein the farnesol analog has a solubility in water that is 10 grams per 100 grams of water or greater.
8. A web comprising a plurality of fibers, wherein the web is coated with a treatment composition, the treatment composition comprising a farnesol analog according to claim 1 .
9. An absorbent article comprising:
a liquid impermeable outer cover;
a liquid permeable bodyside liner, wherein the bodyside liner comprises the web according to claim 8 ; and
an absorbent body disposed between the outer cover and bodyside liner.
10. A method of forming a farnesol analog that is soluble in water from a farnesol molecule having a hydroxyl group, the method comprising:
covalently attaching a hydrophilic end group to the farnesol molecule via reaction with its hydroxyl group to form a covalent linkage, wherein the hydrophilic end group defines a hydroxyl end group, and wherein the covalent linkage comprises an ester group or an ether group, wherein the farnesol analog comprises one of the structures:
where n is an integer from 1 to about 8; m is an integer from 1 to 8; and p is an integer from 1 to 100.
11. The method as in claim 10 , wherein the covalent linkage comprises an ester group formed via an esterification reaction between the hydroxyl group of the farnesol molecule and a carboxylic acid functional molecule.
12. The method as in claim 11 , further comprising:
reacting the carboxylic acid end group with a glycol via a second esterification reaction to form a farnesol analog having a hydroxyl group covalently attached via two ester linkages.
13. The method as in claim 12 , wherein the glycol is selected from the group consisting of ethylene glycol, propylene glycol, and butane-1,4-diol.
14. The method as in claim 10 , wherein the covalent linkage comprises an ether group formed by reacting farnesol with an alcohol via a dehydration reaction to form the ether group.
15. The method as in claim 14 , wherein the alcohol is a glycol selected from the group consisting of ethylene glycol, propylene glycol, and butane-1,4-diol.
16. The method as in claim 14 , wherein the hydrophilic end group comprises a sugar.
17. A wipe comprising the web according to claim 8 .Cited by (0)
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